Friday, January 19, 2018
On December 22, 2017 I went in
for what I thought was my annual CT scan.
I’ve done a lot of these and they are pretty easy. Dr. Ko calls them my “low dose radiation
treatment.” On December 26th I saw
Dr. Bomzer for the follow up appointment.
I see him every six months.
It hadn’t always been like
that. After my surgery on May 19, 2010
to remove the Bronchial Associated
Lymphoid Tumor (BALT), I saw him every three months with CT scans each
time. Gradually they went to every four,
then six. When I asked if it would
eventually be annual visits, he told me “No, we will see each other every six
months forever.” He’s a pretty
conservative doctor, and my colon cancer in 1992 and our family history pretty
much guaranteed close monitoring.. I’m ok
with it.
That surgery went fine. They removed the tumor, analyzed it,
determined that it was cancerous, removed the rest of that half lung, and that
was that.
When I saw Dr. Bomzer on December 26th, 2017, he said
that the radiologist flagged a lesion in my right lung that had changed since
2014. He said that it had definitely
changed since 2010, the first scan that I had.
He said that I needed to see a pulmonologist to determine the next
course of action and referred me to Dr. Al-Saghir.
On January 16th, 2018 Laurie and I went
to see her. The Pulmonology Department
of a hospital has a lot of sick people in it.
There are a lot of oxygen tanks and wheezing. As our friend Pat would say, “There is no
happiness there.” It’s unbelievable that
people still smoke.
Dr. Al-Saghir is quite matter of
fact – no small talk or mincing words, at least during this initial visit. She said that we need to do a biopsy, but the
area in question is in a difficult spot to get to. The fact that the area is small is good for
me, but bad for access. I’ll take
small. Bronchoscopies have improved
quite a lot since 2010, and she may be able to that way, but will need another
CT scan to determine how that could be done.
The alternative is to go surgically through the side into the lung. That poses a higher risk of “lung collapse” –
2 to 4%. That sounded bad to me, but she
said it’s not that big a deal. It would
mean an overnight stay in the hospital, but the lung usually just closes itself
up. Still sounds scary. Both are out-patient procedures and require a
general anesthetic.
Dr. A said there were four possibilities as to what it could
be:
·
Scar tissue.
That seems pretty unlikely to me.
Why would scar tissue grow?
·
Infection.
Also seems unlikely, but what do I know.
They would treat that with some sort of antibiotic.
·
Lymphoma.
That’s what I had before and she said it would probably be treated with
radiation and/or chemotherapy.
·
Lung Cancer.
That would mean surgery. She said
that there is a form of lung cancer that nonsmokers, and some smokers,
get. It’s a less aggressive form that
what smokers typically get.
Dr. Bomzer also mentioned that
whatever I have, it’s “low-grade,”
When you are sitting in a
doctor’s office for an appointment like that, a lot goes through your
mind. You listen, trying to take in the
totality of the discussion, but also trying to hear what isn’t said. But words like “radiation,” “chemotherapy,”
and “lung cancer” have a chilling effect, making it difficult to
concentrate. I had a lot of questions on
the drive home, but couldn’t think of a single one at the time.
When we left her office, Laurie
wanted to go to the gift shop. I knew
she was a little freaked out. She wasn’t
expecting to see and hear what we did. Later
that evening she told me that she could not ask any questions because she was “devastated.”
I had the “high contrast chest
CT scan ” on January 19th. It went quick, as
always. This one was different in that
they took pictures while exhaled and well as with the lungs full, and while I
was on my stomach. The tech said that
the radiologist would ready the scan today and get the results to Dr. Al-Saghir
no later than Tuesday. She said that she
will call me once she has a chance to review them and we’ll determine a course
of action.
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